---
title: "PORTEX Bivona Tracheostomy Silicone Tube, labeled as: a) TTS NEONATAL TRACH T... — FDA record Z-2606-2024 | Is It on Recall"
description: "Smiths Medical has identified that the securement flange of specific lots of the Bivona Neonatal/Pediatric and Adult Tracheostomy products may tear because of a"
url: https://isitonrecall.com/recall/fda-device-z-2606-2024-portex-bivona-tracheostomy-silicone-tube-labeled-as-a-tts-neonatal-trach-tube-product-code-list-numb/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# PORTEX Bivona Tracheostomy Silicone Tube, labeled as: a) TTS NEONATAL TRACH TUBE , Product Code/List Number/Item Code... — FDA record Z-2606-2024

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date May 29, 2024. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: PORTEX Bivona Tracheostomy Silicone Tube, labeled as: a) TTS NEONATAL TRACH TUBE , Product Code/List Number/Item Code 67N025; b) TTS NEONATAL TRACH TUBE , Product Code/List Number/Item Code 67N030; c) TTS NEONATAL TRACH TUBE , Product Code/List Number/Item Code 67N035
- **Reason**: Smiths Medical has identified that the securement flange of specific lots of the Bivona Neonatal/Pediatric and Adult Tracheostomy products may tear because of a manufacturing defect.
- **Classification**: Class I
- **Recalling firm**: Smiths Medical ASD Inc.
- **Quantity**: Not supplied
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2606-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2606-2024%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | a) UDI/DI 15021312006209, Product Code/List Number/Item Code 67N025, Lot Numbers: 3894899, 3949047, 4011355, 4139007, 4153599, 4185400, 4327887, 4331545, 4334876, 4352755, 4353076, 4372094, 4388097, 4400622; b) UDI/DI 15021312006216, Product Code/List Number/Item Code 67N030, Lot Numbers: 3853378, 3868286, 3887733, 3918002, 3939660, 4029491, 4043944, 4051629, 4060201, 4091408, 4113106, 4116109, 4128032, 4148026, 4159991, 4171571, 4185401, 4221331, 4327886, 4331548, 4334878, 4348407, 4374401, 4380992, 4380993, 4389867, 4399126; c) UDI/DI 15021312006223, Product Code/List Number/Item Code 67N035, Lot Numbers: 3868245, 3884266, 3904655, 3923736, 3952406, 3955773, 3961254, 3965335, 4016045, 4016046, 4156603, 4180470, 4216298, 4237347, 4328208, 4334879, 4344968, 4351233, 4362869, 4383593, 4395736 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

Worldwide distribution.

No US distribution state could be established from this record. Check the official notice.

## Dates in the source

- **Report date**: Sep 4, 2024
- **Recall initiation date**: May 29, 2024
- **Center classification date**: Aug 23, 2024

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2606-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Smiths Medical ASD Inc. records](https://isitonrecall.com/brand/smiths-medical-asd-inc/)